Medical Safety Lead

September 3, 2026
Urgent
Application ends: October 3, 2026
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Job Description

๐ŸขCompany: Novartis Healthcare Private Limited
๐Ÿ“Location: Hyderabad, Telangana, India ๐Ÿ‡ฎ๐Ÿ‡ณ
๐Ÿ’ผJob Type: Full-Time, Regular ๐Ÿฅ
๐ŸขWork Mode: Hybrid โ€” 12 days/month in office ๐Ÿ’ป
โณExperience: 3+ years in drug development; 2+ years in patient safety preferred
๐ŸŽ“Education: Pharmacy, Nursing, Pharmacology, Life Sciences or Medical Degree ๐ŸŽ“
๐Ÿ’ฐExpected Salary: โ‚น27 โ€“ โ‚น32 Lakhs Per Year๐Ÿ’ธ
๐Ÿ“ŠJob Category: Healthcare, Medical Safety, Clinical Research, Pharmaceutical, Research & Development ๐ŸŒ
๐ŸŒWebsite: Website
๐Ÿ“žContact: Contact us


๐ŸŒŸWhat if your next career move could combine healthcare expertise with AI?

Patient safety is changing.

Clinical data is growing.
Regulatory requirements are becoming more complex.
And AI is beginning to reshape how safety teams identify risks.

Novartis is hiring a Medical Safety Lead in Hyderabad for professionals who can work at the intersection of clinical safety, drug development, data and technology.


๐ŸŒŸAbout Novartis:
Novartis is a global pharmaceutical company focused on developing innovative medicines that address some of the world’s most challenging healthcare needs.

The company brings together science, technology and healthcare expertise to reimagine medicine and improve patient outcomes. ๐Ÿงฌ

This role sits within the Development organization and focuses on protecting patients throughout the product lifecycle.


๐Ÿ’กAbout the Role:
As a Medical Safety Lead, you’ll be responsible for supporting drug surveillance and clinical safety activities across clinical development and post-marketing programs.

You’ll analyse safety information, evaluate adverse events, identify potential safety signals and contribute to regulatory documentation.

But there’s another interesting layer.

Novartis is looking for professionals who can help apply AI-enabled solutions and AI agents to improve pharmacovigilance processes. ๐Ÿค–

It’s a role where medical expertise meets emerging technology.


๐Ÿ“ŒKey Responsibilities:
๐Ÿ“Œ Monitor clinical safety data, literature, case reports and signal detection activities ๐Ÿ”

๐Ÿ“Œ Conduct medical assessments of individual adverse-event cases

๐Ÿ“Œ Identify, evaluate and monitor safety signals

๐Ÿ“Œ Support regulatory authority responses and healthcare professional safety inquiries

๐Ÿ“Œ Contribute to clinical overviews, summary reports and other safety documents ๐Ÿ“

๐Ÿ“Œ Provide medical input into aggregate safety reports and regulatory submissions

๐Ÿ“Œ Collaborate with global clinical development teams

๐Ÿ“Œ Guide adverse-event coding and causality assessments

๐Ÿ“Œ Interpret clinical safety data and communicate insights to stakeholders

๐Ÿ“Œ Support safety issues, risk escalations, compliance matters and labelling updates

๐Ÿ“Œ Drive the use of AI-enabled solutions to improve pharmacovigilance processes ๐Ÿค–


๐ŸŽฏRequirements:
๐ŸŽฏ Degree in Pharmacy, Nursing, Pharmacology, Life Sciences or Medicine ๐Ÿฉบ

๐ŸŽฏ 3+ years of experience in drug development within a pharmaceutical company

๐ŸŽฏ 2+ years of patient-safety experience is preferred

๐ŸŽฏ Medical degree required for positions involving medical review of individual case safety reports

๐ŸŽฏ Knowledge of clinical trial methodology and regulatory requirements

๐ŸŽฏ Understanding of scientific methodology and statistical principles

๐ŸŽฏ Experience contributing to scientific publications is valuable

๐ŸŽฏ Strong analytical and clinical safety data interpretation skills

๐ŸŽฏ Excellent written and spoken English

๐ŸŽฏ Experience with safety reports and regulatory documentation

๐ŸŽฏ Strong cross-functional communication and issue-management skills


๐ŸŒŸPreferred Skills:
โœ… Pharmacovigilance

โœ… Clinical Safety

โœ… Drug Development

โœ… Adverse Event Assessment

โœ… Signal Detection

โœ… Risk Management

โœ… Regulatory Affairs

โœ… Clinical Trial Methodology

โœ… Safety Reporting

โœ… AI Tools & AI Agents ๐Ÿค–

โœ… Data Analysis

โœ… Scientific Writing


๐ŸŒŸWhy Consider Novartis?
โœ… Work with a global pharmaceutical organization ๐ŸŒ

โœ… Hybrid working model in Hyderabad

โœ… Work on global clinical safety initiatives

โœ… Gain exposure to drug development and regulatory processes

โœ… Work at the intersection of healthcare and AI

โœ… Contribute directly to patient safety

โœ… Collaborate with cross-functional global teams


๐Ÿ”ฅCareer Insight:
The healthcare professionals who stand out tomorrow won’t only understand medicine.

They’ll understand data.

They’ll understand technology.

And increasingly, they’ll understand AI.

Pharmacovigilance is moving beyond traditional case processing toward smarter signal detection, automation and risk intelligence.

If you’re building a career in medical safety, adding technology to your clinical expertise could become one of your biggest advantages.